Why the study?
Congenital venous anomalies can limit standard catheter approaches and distort Koch triangle anatomy, while providers often still rely on fluoroscopy and venography despite 3D imaging availability.
Can non-fluoroscopic catheter ablation be successfully performed in a pediatric patient with AVNRT and atypical venous anatomy?
Can non-fluoroscopic catheter ablation be successfully performed in a pediatric patient with AVNRT and atypical venous anatomy?
Non-fluoroscopic catheter ablation of the slow pathway is feasible and successful even in pediatric patients with atypical venous anatomy.
Supports non-fluoroscopic ablation in select pediatric AVNRT cases; leaves open need for prospective validation before wider adoption.
Catheter ablation of the slow pathway to the atrioventricular node is generally a safe and effective treatment for atrioventricular nodal re-entry tachycardia (AVNRT). However, congenital anomalies of the inferior vena cava and superior draining veins can limit traditional catheter approaches to the right heart from femoral venous access and distort local anatomy within the triangle of Koch, necessitating alternative electrophysiology (EP) mapping and ablation strategies. Despite the widespread availability of non-fluoroscopic 3-dimensional imaging systems, many providers still rely on venography to describe unusual cardiovascular anatomy and fluoroscopy to position EP catheters when mapping and ablating the slow pathway. Herein, we report our experience with a pediatric patient with inducible AVNRT and atypical venous anatomy in whom slow pathway ablation was performed successfully without the use of fluoroscopy. In addition, we describe the modification of a novel mapping technique for targeting the slow pathway for ablation.
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Dasgupta et al. (2022) studied this question.
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